Shah H A, Shipchandler Taha, Vernon Dominic, Baumanis Maraya, Chan David, Nunery William R, Lee Hui Bae Harold
Pediatric Ophthalmology and Adult Strabismus, Illinois Eye and Ear Infirmary, University of Illinois at Chicago, United States.
Otolaryngology and Head and Neck Surgery, Division of Facial Plastic & Reconstructive Surgery, Indiana University School of Medicine, Indianapolis, United States.
Am J Otolaryngol. 2018 Jan-Feb;39(1):34-36. doi: 10.1016/j.amjoto.2017.08.008. Epub 2017 Aug 25.
To report a series of patients with extra-ocular movement restriction and diplopia after orbital fracture repair, and determine the effect of timing of repair and the type of implant used.
A chart review was conducted identifying all patients >18years of age at our institution between June 2005 and June 2008 who underwent orbital fracture repair, and presented with clinically significant diplopia and extra-ocular movement restriction persisting longer than one month after repair. Data collected included timing of repair, implant used within the orbit, and need for revision.
Ten patients were identified with a mean time to primary orbital fracture repair at 9days (range 1-48). Seven patients underwent revision of their orbital fracture repair with removal of the previously placed implant and replacement with non-porous 0.4mm Supramid Foil, whereas one patient underwent lateral and inferior rectus recessions without revision of primary fracture repair. Titanium mesh was the intra-orbital implant found in all patients requiring revision of orbital fracture repair. All revisions resulted in resolution of clinically significant diplopia.
Clinically significant diplopia and extra-ocular movement restriction is not an uncommon complication after orbital fracture repair. In our series, there was a strong association between these complications and the use of porous titanium mesh implants. Revision of fractures significantly improved diplopia in all but one patient. This suggests that meticulous fracture repair and the use of non-porous implants primarily or secondarily may preclude the need for strabismus surgery after orbital trauma.
报告一系列眼眶骨折修复术后出现眼球运动受限和复视的患者,并确定修复时机和所用植入物类型的影响。
对2005年6月至2008年6月期间在本机构接受眼眶骨折修复术、术后出现具有临床意义的复视且眼球运动受限持续超过1个月的所有18岁以上患者进行病历回顾。收集的数据包括修复时机、眼眶内使用的植入物以及是否需要翻修。
确定了10例患者,初次眼眶骨折修复的平均时间为9天(范围1 - 48天)。7例患者对眼眶骨折修复进行了翻修,取出先前放置的植入物,并用无孔0.4mm Supramid箔片替换,而1例患者未对初次骨折修复进行翻修,仅进行了外直肌和下直肌后徙术。钛网是所有需要翻修眼眶骨折修复的患者眼眶内植入物。所有翻修均使具有临床意义的复视得到缓解。
具有临床意义的复视和眼球运动受限是眼眶骨折修复术后并不罕见的并发症。在我们的系列研究中,这些并发症与使用多孔钛网植入物之间存在密切关联。除1例患者外,骨折翻修显著改善了复视。这表明细致的骨折修复以及主要或次要使用无孔植入物可能避免眼眶创伤后斜视手术的需要。